http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103184256-B
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d40285e27f4ed83b8728b0d477404958 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-00 |
filingDate | 2011-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2014-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34e30426652be675bdf9518310ed9295 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37e10bea764ca26b9b327fe3eea35ef3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d1f55d7717057769e3f53c3bf129544 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a129e356b4cc51374de446f93d8a3e8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4ea7754471efb5d0e2765cadb6ad83b |
publicationDate | 2014-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-103184256-B |
titleOfInvention | Method for on-line synthesizing saccharose-6-laurate by lipase catalysis |
abstract | The invention provides a method for on-line synthesizing saccharose-6-laurate by lipase catalysis, comprising: using saccharose and vinyl laurate, with a mol ratio of 1:8-12, as raw materials, using 0.5-10g of Lipozyme TLIM as a catalyst, and using a mixed solvent of tertiary amyl alcohol and DMSO as a reaction solvent, uniformly filling Lipozyme TLIM in a reaction channel of a microfluidic channel reactor, wherein the internal diameter of the reaction channel of the microfluidic channel reactor is 0.8-2.4mm, and the length of the reaction channel is 0.5-1.0m; continuously introducing the raw materials and the reaction solvent into the reaction channel to perform acylation reaction under 40-55 DEG C for 20-35min, on-line collecting the reaction solution, and then obtaining the saccharose-6-laurate after conventional post-treatment on the reaction solution. The method of the invention has advantages of short reaction time, high selectivity and high yield. |
priorityDate | 2011-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 73.